Chemical Formula | C11H10ClN |
Molar Mass | 191.66 g/mol |
Appearance | Solid (predicted, no specific data found) |
Boiling Point | No specific data found |
Melting Point | No specific data found |
Solubility In Water | Low solubility (due to hydrophobic nature of aromatic rings, no exact value found) |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, chloroform (predicted) |
Density | No specific data found |
Vapor Pressure | No specific data found |
Flash Point | No specific data found |
What are the main uses of 4-Chloro-2,8-dimethylquinoline?
4-Chloro-2,8-dimethylquinoline is one of the organic compounds. Its main use is quite extensive and has applications in many fields.
First, in the field of pharmaceutical chemistry, it is often an important synthetic intermediate. Due to the diverse biological activities of quinoline compounds, 4-chloro-2,8-dimethylquinoline can be modified by specific chemical reactions to prepare drugs with antibacterial, anti-inflammatory, anti-tumor and other pharmacological activities. For example, some antibacterial drugs targeting specific bacteria use 4-chloro-2,8-dimethylquinoline as the starting material in the synthesis path. By introducing different functional groups, the interaction between the drug and the bacterial target can be precisely regulated to achieve antibacterial effect.
Second, it also has important uses in materials science. It can be used to synthesize materials with special optical or electrical properties. For example, in the development of some organic Light Emitting Diode (OLED) materials, the introduction of 4-chloro-2,8-dimethylquinoline structural units can improve the luminous efficiency and stability of the materials. Its unique molecular structure can adjust the energy level structure of materials, promoting more effective recombination of electrons and holes, thereby enhancing luminescence properties.
Furthermore, in the field of dye chemistry, 4-chloro-2,8-dimethyl quinoline can be used as a key raw material for the synthesis of new dyes. The conjugated structure of quinoline derivatives endows dyes with good color properties and dyeing fastness. The dyes synthesized on its basis can be used in textile, leather and other industries to dye fabrics and leather with bright and lasting colors.
In summary, 4-chloro-2,8-dimethylquinoline plays an important role in many fields such as medicine, materials, and dyes due to its unique molecular structure and chemical properties, and provides an important material basis for the development of various fields.
What are the physical properties of 4-Chloro-2,8-dimethylquinoline?
4-Chloro-2,8-dimethylquinoline is one of the organic compounds. Its physical properties are particularly important, related to its application and characteristics.
The appearance is usually solid, and the color may be white to light yellow. The characteristics of this color state can be visually identified by the naked eye, and it is quite useful in the preliminary identification of this substance.
The melting point is within a certain range. This value is crucial for determining its purity and the transformation of its material state. When the temperature rises to the melting point, the compound melts from a solid state to a liquid state. This transformation process can be determined by precise experimental instruments.
Furthermore, the boiling point is also one of its important physical properties. The boiling point reflects the temperature required for the substance to change from liquid to gaseous under a specific pressure. Knowing its boiling point helps to grasp the appropriate conditions in chemical operations such as distillation and separation.
In terms of solubility, 4-chloro-2,8-dimethylquinoline has a certain solubility in common organic solvents such as ethanol and ether. However, in water, its solubility is very small. This difference in solubility makes it necessary to consider when separating, purifying and selecting chemical reaction media.
In addition, density is also a property that cannot be ignored. Its density determines the location and distribution of the substance in the mixed system, and plays an important role in understanding the behavior of the substance in operations such as liquid-liquid extraction.
In summary, the physical properties of 4-chloro-2,8-dimethylquinoline, such as appearance, melting point, boiling point, solubility and density, are the basis for in-depth understanding of this substance and its rational application. It is of great significance in many fields such as chemical industry and scientific research.
Is 4-Chloro-2,8-dimethylquinoline chemically stable?
4-Chloro-2,8-dimethylquinoline, which is also an organic compound. The stability of its chemical properties needs to be considered many times.
Looking at its structure, quinoline is a nitrogen-containing heterocyclic aromatic hydrocarbon with certain aromatic properties, which endows it with certain chemical stability. The substitution of the chlorine atom at the 4 position, although the chlorine atom is electron-absorbing, in the quinoline system, the aromatic conjugation system of the quinoline ring is strong, so the effect of the chlorine atom on the overall stability is not severe. The substitution of methyl at the 2,8 positions, with methyl as the power supply group, can increase the electron cloud density of the quinoline ring and slightly increase the stability of the aromatic system.
Under normal conditions, 4-chloro-2,8-dimethylquinoline can maintain a relatively stable state. However, when encountering extreme conditions such as strong oxidants, strong acids, strong bases or high temperatures, the stability may be affected. In case of strong oxidants, the quinoline ring may be oxidized, resulting in structural changes; in case of strong acids and bases, or due to acid-base action, the nitrogen atom is protonated or other reactions occur, destroying the original stable structure of the molecule.
In summary, the chemical properties of 4-chloro-2,8-dimethylquinoline are still stable under conventional mild conditions, but in extremely harsh chemical environments, the stability is difficult to maintain, or various chemical reactions occur, resulting in structural and property changes.
What are the synthesis methods of 4-Chloro-2,8-dimethylquinoline?
The synthesis method of 4-chloro-2,8-dimethylquinoline is quite complicated and has various paths. The following common methods are described in detail.
First, anthranilic acid and 2-chloro-5-methylacetophenone are used as starting materials. Under appropriate conditions, such as in a specific solvent, with a suitable catalyst, the condensation reaction is carried out first. During condensation, factors such as temperature and reaction time need to be carefully regulated. If the temperature is too high, side reactions may occur; if the temperature is too low, the reaction will be delayed. After the condensation is completed, the obtained product can be cyclized to form the prototype of 4-chloro-2,8-dimethylquinoline. However, this process requires careful selection of cyclization reagents and reaction conditions to ensure the purity and yield of the product.
Second, m-chloroaniline and acetylacetone are used as starting materials. The two first undergo a series of reactions to generate a specific intermediate product. This reaction requires precise control of the proportion of reactants, the proportion is unbalanced, or the subsequent reaction process is affected. Subsequently, the intermediate product is cyclized and methylated under appropriate reagents and conditions. During the methylation process, the choice and dosage of methylation reagents are extremely critical. Improper dosage or the degree of methylation does not match expectations, affecting the structure and purity of the final product. Through this series of reactions, 4-chloro-2,8-dimethylquinoline can also be obtained.
Third, with the help of Friedländer synthesis method. The corresponding o-halobenzaldehyde and 2-amino-3-methylpyridine derivatives are used as raw materials. Under suitable alkaline conditions and catalysts, the condensation and cyclization reactions gradually occur. During the reaction process, the strength of alkalinity has a great influence on the reaction rate and direction. If the alkalinity is too strong, or the structure of the reactants is destroyed; if the alkalinity is too weak, the reaction is difficult to start. Through the fine control of each link of this method, it is also an effective way to synthesize 4-chloro-2,8-dimethylquinoline.
All the above synthesis methods have their own advantages and disadvantages. In practical application, the appropriate method should be carefully selected according to specific requirements, such as product purity, cost, difficulty of reaction conditions, etc., and each reaction step should be carefully regulated to achieve the ideal synthesis effect.
What are the precautions for 4-Chloro-2,8-dimethylquinoline in storage and transportation?
4-Chloro-2,8-dimethylquinoline is an organic compound. When storing and transporting, many matters need to be paid attention to.
First words storage, this compound should be placed in a cool, dry and well ventilated place. Cover because of its nature or affected by temperature and humidity, if it is placed in a high temperature and humid place, it may cause deterioration. And it needs to be kept away from fire and heat sources, because it may be flammable, it is easy to cause danger in case of open flames and hot topics. It must be stored separately from oxidizing agents, acids, bases, etc., and must not be mixed to prevent chemical reactions and dangerous accidents. The storage area should also be prepared with suitable materials to contain leaks, in case of leakage, it can be dealt with in time, and will not spread.
As for transportation, it is necessary to ensure that the packaging is complete and sealed before transportation. During transportation, it should be stably loaded and unloaded to prevent damage to packaging and containers. Transportation vehicles should be equipped with corresponding types and quantities of fire-fighting equipment and leakage emergency treatment equipment. When driving, follow the specified route and do not stop in densely populated areas and places with open flames. If it is road transportation, dangerous goods signs should be posted according to regulations and traffic rules should be followed to ensure transportation safety. Do not mix with contraindicated substances to avoid accidents due to interaction on the way. In this way, it is necessary to ensure that 4-chloro-2,8-dimethylquinoline is safe during storage and transportation.